Canonical Allele Identifier: CA96921693

Gene: KDR

Linked Data

• dbSNP Id: rs1011816605
• MyVariant Identifiers: chr4:g.55991473G>C (hg19) ; chr4:g.55125306G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55125306G>C , CM000666.2:g.55125306G>C	GRCh38
NC_000004.11:g.55991473G>C , CM000666.1:g.55991473G>C	GRCh37
NC_000004.10:g.55686230G>C	NCBI36
NG_012004.1:g.5290C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.-13C>G MANE Select	ENSP00000263923.4:n.-13C>G
ENST00000263923.4:c.-13C>G	ENSP00000263923.4:n.-13C>G
NM_002253.2:c.-13C>G	NP_002244.1:n.-13C>G
NM_002253.3:c.-13C>G	NP_002244.1:n.-13C>G
NM_002253.4:c.-13C>G MANE Select	NP_002244.1:n.-13C>G